Years of Experience
Pharmaceutical CDMO Excellence • Est. 2008Global Pharmaceutical CDMO & Effervescent Specialists
Established in 2008 in Ranoli, Vadodara, Vovantis Laboratories is a specialized research-driven Contract Development and Manufacturing Organization (CDMO). We engineer water-soluble, effervescent, and specialized solid oral formulations that deliver enhanced bioavailability, stability, and patient compliance.
Proprietary R&D
Advanced kinetics, taste masking, and rapid effervescent dispersion modeling.
USFDA & cGMP Rigor
Continuous quality compliance adhering strictly to international pharmacopoeias.
Years of Excellence
Manufacturing and CDMO leadership since 2008
Global Export Markets
Supplying pharmaceutical brands worldwide
Annual Tablet Capacity
High-speed rotary presses & automated packaging
Regulatory Compliance
USFDA & WHO-GMP compliant plant audits
Featured Products & Formulations
Explore commercialized formulation dossiers engineered for rapid dissolution kinetics, tropical stability (Zone IVb), and international pharmacopoeial compliance.
Pharmaceutical & Engineering Excellence
Uncompromising cGMP quality standards, advanced effervescent technologies, and state-of-the-art automated manufacturing infrastructure.
Excellence in Effervescent Production
Unit 1 & Unit 2 Audited Facilities
Ranoli Vadodara Campus & Manufacturing Prowess
Located in Gujarat's pharmaceutical manufacturing corridor, Vovantis operates a purpose-built USFDA and WHO-GMP audited manufacturing campus. Specially engineered HVAC networks maintain relative humidity below 20% across all granulation, tableting, and packaging suites.
- Completely isolated granulation suites with dynamic air-locks
- Automated moisture-barrier Alu-Alu blisters & desiccant tube lines
- Real-time environmental monitoring with BMS automation
Class 100,000 / ISO 8
Positive pressure HEPA-filtered cleanroom suites (EU-GMP Grade D) engineered with automated interlocking airlocks and personnel air-showers for strict particulate isolation.
Low RH Climate Suites
Dedicated industrial desiccant dehumidification network maintaining moisture-critical effervescent environmental boundaries from granulation to primary filling.
High-Speed Rotary Compression
Automated multi-station high-tonnage rotary tablet presses featuring in-process automated weight regulation, continuous hardness monitoring, and rapid tooling changes.
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QA/QC Analytical Laboratory
Comprehensive in-house HPLC, GC, dissolution apparatus, FTIR spectroscopy, and walk-in ICH stability chambers qualified for Zone IVb global climate testing.
Comprehensive CDMO Solutions & Contract Manufacturing
From innovative molecule formulation to global commercial release, Vovantis delivers world-class manufacturing, analytical rigor, and tailored private-label solutions.
Effervescent Tableting
Specialized formulation, precision humidity control, and high-speed rotary compression for rapid effervescence, crystal-clear dissolution, and superior bioavailability.
Explore Effervescent Systems
Formulation R&D & Scale-Up
In-house scientists specialize in API compatibility, dissolution kinetics, custom flavor profiling, and stability modeling for new chemical entities and generic line extensions.
Explore Formulation R&D
Solid Oral Dosage Forms
Full-scale commercial production of chewable, dispersible, and sublingual tablets engineered for rapid therapeutic onset and effortless patient swallowing.
View Solid Oral Dosages
Nutraceuticals & Supplements
Turnkey dietary formulations including high-potency Vitamin C, Zinc, multi-minerals, hydration electrolytes, and botanical extracts in effervescent dosage formats.
Explore 113+ Formulations
Packaging & Barrier Solutions
Automated high-speed tube filling with integrated silica desiccant stoppers, as well as Alu-Alu and tropical blister lines ensuring long-term shelf stability in Zone IVb climates.
Contract Manufacturing & Packaging
Global Regulatory Dossiers
Comprehensive CTD/eCTD dossier compilation, real-time and accelerated stability studies (ICH guidelines), analytical method validation, and global regulatory registration support.
Regulatory Dossier InquiriesStart Your CDMO Project
Accelerate your solid oral or effervescent pipeline from initial formulation feasibility to commercial-scale manufacturing with Vovantis.